Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism

Stefania Fornarino, Michela Stagnaro, Martina Rinelli, Francesco Danilo Tiziano, Margherita M. Mancardi, Maria Traverso, Edvige Veneselli, Elisa De Grandis

Risultato della ricerca: Contributo in rivistaArticolo in rivista

9 Citazioni (Scopus)


Genetic research has shown that mutations that modify the protein-coding sequence of ATP1A3, the gene encoding the α3 subunit of Na(+)/K(+)-ATPase, cause both rapid-onset dystonia parkinsonism and alternating hemiplegia of childhood. These discoveries link two clinically distinct neurological diseases to the same gene, however, ATP1A3 mutations are, with one exception, disease-specific. Although the exact mechanism of how these mutations lead to disease is still unknown, much knowledge has been gained about functional consequences of ATP1A3 mutations using a range of in-vitro and animal model systems, and the role of Na(+)/K(+)-ATPases in the brain. Researchers and clinicians are attempting to further characterise neurological manifestations associated with mutations in ATP1A3, and to build on the existing molecular knowledge to understand how specific mutations can lead to different diseases.
Lingua originaleEnglish
pagine (da-a)2037-2038
Numero di pagine2
Stato di pubblicazionePubblicato - 2014


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